LEICA Surgipath EA-50 Modified - Indonesia BPOM Medical Device Registration
LEICA Surgipath EA-50 Modified is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10201220333. The device is manufactured by LEICA BIOSYSTEMS RICHMOND, INC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is BIOGEN SCIENTIFIC.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
LEICA BIOSYSTEMS RICHMOND, INCCountry of Origin
United States
Authorized Representative
BIOGEN SCIENTIFICAR Address
Rukan Tanjung Mas Raya Jl.Raya Lenteng Agung Blok B1 No.21
Registration Date
Oct 10, 2023
Expiry Date
Jun 30, 2025
Product Type
Biological Dyes
Dye and chemical solution stains.
Invitro Diagnostics
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